Canonical Allele Identifier: CA415287667

Gene: NSDHL

Linked Data

• MyVariant Identifiers: chrX:g.152037623C>G (hg19) ; chrX:g.152869079C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152869079C>G , CM000685.2:g.152869079C>G	GRCh38
NC_000023.10:g.152037623C>G , CM000685.1:g.152037623C>G	GRCh37
NC_000023.9:g.151788279C>G	NCBI36
NG_009163.1:g.43113C>G
NG_009163.2:g.43113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370274.8:c.1085C>G MANE Select	ENSP00000359297.3:p.Thr362Ser
ENST00000370274.7:c.1085C>G	ENSP00000359297.3:p.Thr362Ser
ENST00000440023.5:c.1085C>G	ENSP00000391854.1:p.Thr362Ser
NM_001129765.1:c.1085C>G	NP_001123237.1:p.Thr362Ser
NM_015922.2:c.1085C>G	NP_057006.1:p.Thr362Ser
XM_011531178.1:c.1085C>G	XP_011529480.1:p.Thr362Ser
XM_011531178.2:c.1085C>G	XP_011529480.1:p.Thr362Ser
XM_017029564.1:c.1133C>G	XP_016885053.1:p.Thr378Ser
NM_015922.3:c.1085C>G MANE Select	NP_057006.1:p.Thr362Ser
NM_001129765.2:c.1085C>G	NP_001123237.1:p.Thr362Ser